WO2018230274A1 - Endoscope - Google Patents

Endoscope Download PDF

Info

Publication number
WO2018230274A1
WO2018230274A1 PCT/JP2018/019596 JP2018019596W WO2018230274A1 WO 2018230274 A1 WO2018230274 A1 WO 2018230274A1 JP 2018019596 W JP2018019596 W JP 2018019596W WO 2018230274 A1 WO2018230274 A1 WO 2018230274A1
Authority
WO
WIPO (PCT)
Prior art keywords
distal end
end side
imaging
imaging unit
endoscope
Prior art date
Application number
PCT/JP2018/019596
Other languages
French (fr)
Japanese (ja)
Inventor
啓介 天野
Original Assignee
オリンパス株式会社
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by オリンパス株式会社 filed Critical オリンパス株式会社
Publication of WO2018230274A1 publication Critical patent/WO2018230274A1/en
Priority to US16/708,716 priority Critical patent/US20200107708A1/en

Links

Images

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B1/00Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor
    • A61B1/00163Optical arrangements
    • A61B1/00174Optical arrangements characterised by the viewing angles
    • A61B1/00179Optical arrangements characterised by the viewing angles for off-axis viewing
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B1/00Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor
    • A61B1/00064Constructional details of the endoscope body
    • A61B1/00071Insertion part of the endoscope body
    • A61B1/0008Insertion part of the endoscope body characterised by distal tip features
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B1/00Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor
    • A61B1/00064Constructional details of the endoscope body
    • A61B1/00071Insertion part of the endoscope body
    • A61B1/0008Insertion part of the endoscope body characterised by distal tip features
    • A61B1/00096Optical elements
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B1/00Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor
    • A61B1/00131Accessories for endoscopes
    • A61B1/00137End pieces at either end of the endoscope, e.g. caps, seals or forceps plugs
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B1/00Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor
    • A61B1/00163Optical arrangements
    • A61B1/00165Optical arrangements with light-conductive means, e.g. fibre optics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B1/00Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor
    • A61B1/00163Optical arrangements
    • A61B1/00165Optical arrangements with light-conductive means, e.g. fibre optics
    • A61B1/00167Details of optical fibre bundles, e.g. shape or fibre distribution
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B1/00Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor
    • A61B1/012Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor characterised by internal passages or accessories therefor
    • A61B1/018Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor characterised by internal passages or accessories therefor for receiving instruments
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B1/00Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor
    • A61B1/04Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor combined with photographic or television appliances
    • A61B1/05Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor combined with photographic or television appliances characterised by the image sensor, e.g. camera, being in the distal end portion
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B8/00Diagnosis using ultrasonic, sonic or infrasonic waves
    • A61B8/12Diagnosis using ultrasonic, sonic or infrasonic waves in body cavities or body tracts, e.g. by using catheters

Definitions

  • the present invention relates to an endoscope.
  • endoscopes have been widely used for various examinations in the medical field and the industrial field.
  • medical endoscopes obtain in-vivo images in a body cavity without incising the subject by inserting an insertion unit provided with an imaging unit into the body cavity of the subject such as a patient. it can.
  • the medical endoscope can perform a therapeutic treatment by protruding a treatment tool from the distal end side of the insertion portion. For these reasons, it is widely used.
  • an imaging hole for disposing an imaging unit, a treatment instrument insertion passage, and the like are adjacent to each other in a distal end rigid member provided on the distal end side of the insertion portion. Is formed. On the distal end surface of the distal rigid member, a treatment instrument projecting port for projecting the treatment instrument inserted into the treatment instrument insertion path into the subject is formed.
  • the imaging lens of the imaging unit disposed in the imaging hole is provided so as to be exposed from the distal end surface of the distal end hard member.
  • the imaging unit When assembling the insertion portion of the endoscope, the imaging unit is inserted from the proximal end side of the imaging hole, and the abutting portion provided on the distal end side of the imaging unit is provided on the distal end side of the imaging hole.
  • the imaging unit is positioned with respect to the distal end hard member so that the position of the imaging lens with respect to the distal end surface of the distal end hard member becomes a predetermined position by being abutted against the abutting surface.
  • the abutting surface is provided on the distal end side of the imaging unit, there may arise a problem that the diameter of the distal end hard member is prevented from being reduced.
  • the present invention has been made in view of the above problems, and an object of the present invention is to provide an endoscope capable of positioning an imaging unit with respect to the distal end hard member while reducing the diameter of the distal end side of the distal end hard member. Is to provide.
  • an endoscope has a lens unit and an image transmission unit, and is inserted into the subject, an imaging unit that images the subject.
  • a distal end rigid member provided with a groove on the proximal end side of the imaging hole; and an abutting portion provided on the proximal end side in the distal end hard member of the imaging unit and abutting against the distal end side end surface of the groove. It is characterized by comprising.
  • the image transmission unit includes an image transmission member and a base provided on a distal end side of the image transmission member.
  • the abutting portion is provided separately on the outer peripheral surface of the base.
  • the endoscope according to the present invention is characterized in that, in the above invention, the abutting portion is a C-ring.
  • the endoscope according to the present invention is characterized in that, in the above invention, the C-ring is fixed to the base by adhesion.
  • the image transmission member includes an image guide bundle in which a plurality of image guide fibers are bundled, or an imaging element and a signal line. It is what.
  • the thickness between the imaging hole of the distal end hard member and the treatment instrument insertion path is the distal side in the axial direction of the distal end hard member. It changes from the base end side, The front end side end surface of the said groove part is located in the base end side rather than the location where the said thickness is the thinnest.
  • the endoscope according to the present invention has an effect that the imaging unit can be positioned with respect to the hard tip member while reducing the diameter of the hard tip member.
  • FIG. 1 is a diagram schematically illustrating an endoscope system according to the first embodiment.
  • FIG. 2 is a perspective view schematically showing a distal end configuration of an insertion portion of the ultrasonic endoscope according to the first embodiment.
  • FIG. 3 is a partial cross-sectional view schematically showing the distal end configuration of the insertion portion of the ultrasonic endoscope according to the first embodiment.
  • FIG. 4 is a perspective view showing the imaging unit according to the first embodiment.
  • FIG. 5 is a perspective view of a C-ring provided in the imaging unit.
  • FIG. 6 is a cross-sectional view of the IG bundle base as viewed from the axial direction of the IG bundle base in a state where the C ring is provided.
  • FIG. 1 is a diagram schematically illustrating an endoscope system according to the first embodiment.
  • FIG. 2 is a perspective view schematically showing a distal end configuration of an insertion portion of the ultrasonic endoscope according to the first embodiment.
  • FIG. 7 is an enlarged view of the imaging unit in the distal end hard member of the ultrasonic endoscope according to the first embodiment and the vicinity thereof.
  • FIG. 8 is an enlarged view of the imaging unit and the vicinity thereof in the distal end hard member of the ultrasonic endoscope according to the comparative example.
  • FIG. 9 is a perspective view illustrating another example of the imaging unit.
  • FIG. 10 is a perspective view of a semi-tubular member provided in the imaging unit.
  • FIG. 11 is a cross-sectional view seen from the axial direction of the IG bundle base in a state where the semi-tubular member is provided on the IG bundle base.
  • FIG. 12 is an enlarged view of another example of the imaging unit and its vicinity in the distal end hard member of the ultrasonic endoscope according to the first embodiment.
  • FIG. 13 is a diagram illustrating a case where a prismatic member is provided as an abutting portion on the outer peripheral surface of the IG bundle base.
  • FIG. 14 is a diagram showing a case where an inverted concave member is provided as an abutting portion on the outer peripheral surface of the IG bundle base.
  • FIG. 15 is an enlarged view of the imaging unit and the vicinity thereof in the distal end rigid member of the ultrasonic endoscope according to the second embodiment.
  • FIG. 1 is a diagram schematically showing an endoscope system 1 including an ultrasonic endoscope 2 according to the first embodiment.
  • an endoscope system 1 according to Embodiment 1 includes an ultrasonic endoscope 2, an ultrasonic observation device 3, an endoscope observation device 4, a display device 5, and a light source device.
  • 6 is a system for performing ultrasonic diagnosis in a subject such as a person using the ultrasonic endoscope 2.
  • the ultrasonic endoscope 2 converts an electrical pulse signal received from the ultrasonic observation apparatus 3 into an ultrasonic pulse (acoustic pulse) and irradiates the subject with an ultrasonic transducer provided at the tip thereof. At the same time, the ultrasonic echo reflected from the subject is converted into an electrical echo signal expressed by a voltage change and output.
  • the ultrasound endoscope 2 includes an imaging unit 300 (see FIG. 3) that performs optical imaging, and the subject's digestive tract (esophagus, stomach, duodenum, large intestine), or respiratory organ (trachea, bronchus). It is possible to take images of the digestive tract and respiratory organs. In addition, surrounding organs (pancreas, gallbladder, bile duct, biliary tract, lymph node, mediastinal organ, blood vessel, etc.) can be imaged using ultrasound.
  • the ultrasonic endoscope 2 has a light guide that guides illumination light to be irradiated onto the subject during imaging by the imaging unit 300.
  • the light guide has a distal end portion reaching the distal end of the insertion portion 21 to the subject of the ultrasonic endoscope 2, and a proximal end portion connected to the light source device 6 that generates illumination light.
  • the ultrasonic endoscope 2 includes an insertion portion 21, an operation portion 22, a universal cord 23, and a connector 24.
  • the insertion part 21 is a part inserted into the subject.
  • the insertion portion 21 is provided on the distal end side, a distal end hard member 211 that holds the ultrasonic transducer 7, and a bending portion that is connected to the proximal end side of the distal end hard member 211 and can be bent.
  • 212 and a flexible tube portion 213 connected to the proximal end side of the bending portion 212 and having flexibility.
  • the ultrasonic transducer 7 As the ultrasonic transducer 7, a plurality of piezoelectric elements are provided in an array, and the piezoelectric elements involved in transmission / reception are electronically switched, or the transmission / reception of each piezoelectric element is delayed.
  • a convex type is employed in which scanning is performed electronically by applying the
  • the method of the ultrasonic transducer 7 is not limited to the convex type, and may be a radial type or a linear type.
  • a light guide that transmits illumination light supplied from the light source device 6 and a plurality of signal cables that transmit various signals are routed inside the insertion portion 21.
  • a treatment instrument insertion passage 219 (see FIG. 3) for inserting a treatment instrument such as forceps is formed.
  • the operation unit 22 is a part that is connected to the proximal end side of the insertion unit 21 and receives various operations from a doctor or the like. As shown in FIG. 1, the operation unit 22 includes a bending knob 221 for performing a bending operation on the bending unit 212 and a plurality of operation members 222 for performing various operations. In addition, the operation section 22 is formed with a treatment instrument insertion port 223 that communicates with the treatment instrument insertion path 219 (see FIG. 3) and allows the treatment instrument to be inserted into the treatment instrument insertion path 219.
  • the universal cord 23 is a cable that extends from the operation unit 22 and includes a plurality of signal cables that transmit various signals, a light guide that transmits illumination light supplied from the light source device 6, and the like.
  • the connector 24 is provided at the tip of the universal cord 23, and the first connector part 241, the second connector part 242, and the third connector to which the ultrasonic cable 31, the video cable 41, and the light source device 6 are connected, respectively.
  • a connector portion 243 is provided.
  • the ultrasonic observation apparatus 3 is electrically connected to the ultrasonic endoscope 2 via the ultrasonic cable 31 and outputs a pulse signal to the ultrasonic endoscope 2 via the ultrasonic cable 31 and is supersonic.
  • An echo signal is input from the sonic endoscope 2. Then, the ultrasonic observation device 3 performs a predetermined process on the echo signal to generate an ultrasonic image.
  • the endoscope observation apparatus 4 is electrically connected to the ultrasonic endoscope 2 via a video cable 41, and an image signal from the ultrasonic endoscope 2 is input via the video cable 41. Then, the endoscope observation apparatus 4 performs a predetermined process on the image signal to generate an endoscope image.
  • the display device 5 is configured by using a liquid crystal or organic EL (Electro Luminescence), a projector, a CRT (Cathode Ray Tube), etc., and an ultrasonic image generated by the ultrasonic observation device 3 or an endoscope observation. An endoscopic image generated by the apparatus 4 is displayed.
  • a liquid crystal or organic EL Electro Luminescence
  • a projector a projector
  • a CRT Cathode Ray Tube
  • the light source device 6 supplies illumination light for illuminating the inside of the subject to the ultrasonic endoscope 2.
  • FIG. 2 is a perspective view showing a distal end configuration of the insertion portion 21 of the ultrasonic endoscope 2 according to the first embodiment.
  • FIG. 3 is a partial cross-sectional view showing the distal end configuration of the insertion portion 21 of the ultrasonic endoscope 2 according to the first embodiment.
  • illustration of wiring connected to the ultrasonic transducer module 214 is omitted.
  • the distal end side of the insertion portion 21 includes an ultrasonic transducer module 214 that holds the ultrasonic transducer 7 and an endoscope module 215.
  • an illumination lens 215a constituting the illumination unit, an observation window 215b constituting the imaging unit 300, and a treatment tool protrusion for projecting a treatment tool such as forceps are projected.
  • a mouth 215c is provided.
  • an imaging hole 216 for arranging the imaging unit 300 is provided to be inclined with respect to the longitudinal axis direction of the insertion portion 21.
  • a treatment instrument insertion passage 219 communicating with the treatment instrument protrusion 215c is provided in the distal end hard member 211, and the vicinity of the end portion of the treatment instrument insertion passage 219 connected to the treatment instrument protrusion 215c is the distal end. It is inclined upward with respect to the axial direction of the hard member 211, and the treatment instrument is provided so as to protrude in a direction inclined upward with respect to the axial direction from the treatment instrument protrusion 215c.
  • the axial direction of the distal end hard member 211 referred to here is a direction along the longitudinal direction when the insertion portion 21 is straightened.
  • “above the distal end rigid member 211 in the axial direction” means that the treatment instrument insertion path 219 is located above the imaging unit 300 and the ultrasonic transducer module 214 is located below the imaging unit 300.
  • the endoscope module 215 is located at the position shown in FIGS. 2 and 3.
  • the imaging unit 300 includes a lens unit 310 and an image guide bundle unit (hereinafter referred to as an IG bundle unit) 320 that is an image transmission unit.
  • the image transmission unit may be configured by an image sensor such as a CCD (Charge Coupled Device) or CMOS (Complementary Metal Oxide Semiconductor) and a signal line.
  • CCD Charge Coupled Device
  • CMOS Complementary Metal Oxide Semiconductor
  • the lens unit 310 is configured by holding a plurality of lenses such as an observation window 215b and objective lenses 311 and 312 in a lens frame 313 that is a cylindrical member.
  • the tip of a guide fiber (hereinafter referred to as IG fiber) is abutted. Further, the proximal end side of the lens frame 313 is fixed to the distal end side of the IG bundle base 322 with an adhesive.
  • the IG bundle unit 320 includes an image guide bundle (hereinafter referred to as an IG bundle) 321 in which a plurality of IG fibers guided to the operation unit 22 through the bending portion 212 and the flexible tube portion 213, and the IG bundle.
  • An IG bundle base 322 which is a cylindrical member including the distal end side of the 321 and a flexible tube 323 including a base end side of the IG bundle base 322 of the IG bundle 321 are provided.
  • FIG. 4 is a perspective view showing the imaging unit 300 according to the first embodiment.
  • FIG. 5 is a perspective view of the C ring 324 provided in the imaging unit 300.
  • FIG. 6 is a cross-sectional view seen from the axis direction of the IG bundle base when the C ring 324 is provided on the IG bundle base 322.
  • a C ring 324 as shown in FIG. 5 is used as the abutting portion for positioning the imaging unit 300 with respect to the distal end hard member 211, and the distal end rigid member of the imaging unit 300.
  • the base end side in 211 specifically, as shown in FIGS. 4 and 6, is provided on the outer peripheral surface of the IG bundle base 322 separately from the IG bundle base 322.
  • the C ring 324 is fixed to the outer peripheral surface of the IG bundle base 322 with an adhesive.
  • the C ring 324 is made of a metal such as stainless steel, titanium, a titanium alloy, and a Cu—Zn alloy (brass).
  • the C ring 324 may be fixed to the outer peripheral surface of the IG bundle base 322 by welding instead of an adhesive. Further, the abutting portion may be provided integrally with the IG bundle base 322 and provided on the outer peripheral surface of the IG bundle base 322.
  • FIG. 7 is an enlarged view of the imaging unit 300 and its vicinity in the distal end hard member 211 of the ultrasonic endoscope 2 according to the first embodiment.
  • illustration of wiring connected to the ultrasonic transducer module 214 is omitted.
  • a step where the C ring 324 provided on the outer peripheral surface of the IG bundle base 322 abuts is formed on the inner wall surface on the proximal end side of the imaging hole 216.
  • This step is formed by providing a groove 217 through which the C-ring 324 provided in the IG bundle base 322 can pass along the axial direction of the imaging hole 216 on the inner wall surface on the proximal end side of the imaging hole 216.
  • the base end side end surface of the groove portion 217 is open, and the front end side end surface of the groove portion 217 forms an abutting surface 217 a that abuts against the front end side end surface 324 a of the C ring 324. Then, the imaging unit 300 is positioned with respect to the distal end hard member 211 by abutting the abutting surface 217a provided in the groove 217 and the distal end side end surface 324a of the C ring 324 provided in the IG bundle base 322.
  • the positioning of the imaging unit 300 with respect to the distal end hard member 211 in the first embodiment refers to the imaging of the observation window 215b provided in the lens unit 310 of the imaging unit 300 with respect to the distal end inclined surface of the distal end hard member 211. That is, the imaging unit 300 is assembled to the distal end hard member 211 so as to be located at a predetermined position where it does not go out or enter too much from the opening on the distal end side of the hole 216.
  • a bending portion 219 a for bending the treatment instrument insertion path 219 is provided, and the treatment instrument insertion path with respect to the imaging hole 216 is provided.
  • 219 is inclined so as to approach the imaging hole 216 from the base end side toward the bent portion 219a side, and away from the imaging hole 216 from the bent portion 219a toward the distal end side (the treatment instrument protrusion port 215c side). So as to be inclined.
  • the thickness between the imaging hole 216 of the distal end rigid member 211 and the treatment instrument insertion path 219 changes from the distal end side to the proximal end side, and the thickness is increased at the portion where the bent portion 219a is located. Becomes the thinnest.
  • the groove portion 217 is formed so that the abutting surface 217a is positioned closer to the base end side than the thinnest portion (the portion where the bent portion 219a is located) in the distal end hard member 211.
  • a C ring 324 is provided on the outer peripheral surface of the IG bundle base 322 in correspondence with the position of the abutting surface 217a.
  • FIG. 8 is an enlarged view of the imaging unit 300 and its vicinity in the distal end hard member 211 of the ultrasonic endoscope 2 according to the comparative example.
  • illustration of wiring connected to the ultrasonic transducer module 214 is omitted.
  • the abutting portion 314 is provided integrally with the lens frame 313 on the distal end side in the distal end hard member 211 of the imaging unit 300, specifically, on the lens frame 313. Further, when the imaging unit 300 is inserted into the imaging hole 216 from the proximal end side of the distal end hard member 211, a groove 218 through which the abutting part 314 provided in the lens frame 313 can pass is formed in the imaging hole 216.
  • the imaging unit 300 is positioned with respect to the distal end hard member 211 by abutting the abutting surface 218a which is the distal end side end surface of the groove portion 218 and the distal end side end surface 314a of the abutting portion 314 provided on the lens frame 313. Is made.
  • the thickness in the thinnest portion is the depth of the groove portion 218.
  • the durability of the distal end hard member 211 is reduced.
  • the groove portion 217 extends to the thinnest portion (the portion where the bent portion 219a of the treatment instrument insertion path 219 is located). Therefore, it can be suppressed that the thickness of the tip hard member 211 is deteriorated because the thickness is too thin.
  • an imaging unit for the distal end hard member 211 while reducing the diameter on the distal end side of the distal end hard member 211 300 positionings can be performed.
  • the groove portion 217 is formed over the entire circumference in the circumferential direction of the inner wall surface on the proximal end side of the imaging hole 216.
  • the imaging unit 300 when the imaging unit 300 is assembled to the distal end hard member 211, the imaging unit 300 is rotated in the imaging hole 216 in order to adjust the resolution due to the arrangement direction of the IG fibers of the IG bundle unit 320. Let Therefore, the groove portion 217 is formed over the entire circumference in the circumferential direction of the inner wall surface on the proximal end side of the imaging hole 216, so that the abutting surface 217a is provided over the entire circumference in the circumferential direction of the inner wall surface.
  • the imaging unit 300 can be positioned with respect to the distal end hard member 211.
  • the observation window 215b and the objective lens 311 are disposed at the end of the lens frame 313 on the front end side.
  • the IG bundle 321 is disposed in the IG bundle base 322 so that the opening on the front end side of the IG bundle base 322 and the front end of the IG fiber constituting the IG bundle 321 are flush with each other.
  • the IG bundle 321 are fixed with an adhesive or the like.
  • the IG bundle 321 is provided with a flexible tube 323 in advance, except for a portion where the tip side IG bundle base 322 is provided.
  • the surface of the base end side of the objective lens 312 constituting the lens unit 310 and the tip of the IG fiber disposed in the IG bundle base 322 are brought into contact with each other, so that the objective lens 312 is brought into contact with the tip of the IG bundle base 322. Fix to the side edge with adhesive.
  • the distal end portion of the IG bundle unit 320 to which the objective lens 312 is fixed in this manner is inserted into the lens frame 313 from the proximal end side opening of the lens frame 313.
  • the IG bundle unit 320 is moved back and forth in the lens frame 313 to adjust the distance between the objective lens 311 and the objective lens 312, and after performing optical adjustment such as focus adjustment, the IG bundle unit 320 is moved toward the lens frame 313.
  • the bundle base 322 is bonded and fixed with an adhesive or the like.
  • the C ring 324 is fixed to the outer peripheral surface of the IG bundle base 322 with an adhesive or the like at a predetermined distance from the tip of the lens unit 310. Then, the imaging unit 300 is inserted into the imaging hole 216 from the base end side of the distal end hard member 211, and the C ring 324 is formed on the abutting surface 217a through the groove portion 217 formed on the inner wall surface on the base end side of the imaging hole 216. The imaging unit 300 is positioned with respect to the distal end hard member 211 by abutting against the distal end side end surface 324a.
  • the imaging unit 300 is placed in the imaging hole 216 in order to adjust the resolution caused by the arrangement direction of the IG fibers of the IG bundle unit 320. Rotate. Then, after the resolution is adjusted, the imaging unit 300 is fixed to the distal end hard member 211 with an adhesive or the like, whereby the assembly of the imaging unit 300 to the distal end hard member 211 is completed.
  • FIG. 9 is a perspective view showing another example of the imaging unit 300.
  • FIG. 10 is a perspective view of the semi-tubular member 325 provided in the imaging unit 300.
  • FIG. 11 is a cross-sectional view as viewed from the axial direction of the IG bundle base in a state where the semi-tubular member 325 is provided on the IG bundle base 322.
  • FIG. 12 is an enlarged view of another example of the imaging unit 300 and the vicinity thereof in the distal end hard member 211 of the ultrasonic endoscope 2 according to the first embodiment. In FIG. 12, illustration of wiring connected to the ultrasonic transducer module 214 is omitted.
  • a semi-tubular member 325 as shown in FIG. 10 is used instead of the C ring 324 as the abutting portion provided in the IG bundle base 322.
  • the semi-tubular member 325 is provided separately from the IG bundle base 322 on the outer peripheral surface of the IG bundle base 322, and the IG bundle base 322 and the semi-tubular member 325 are fixed by an adhesive.
  • the front end side end surface 325 a of the semi-tubular member 325 is abutted against the abutting surface 217 a of the imaging hole 216, and the imaging unit 300 is positioned with respect to the distal end hard member 211.
  • the groove portion 217 extends substantially over the entire circumference in the circumferential direction of the inner wall surface on the proximal end side of the imaging hole 216.
  • the groove 217 may be formed in a semicircular shape only on the treatment instrument insertion passage 219 side in the circumferential direction of the inner wall surface.
  • the imaging unit 300 is rotated about the axis, and each IG fiber of the IG bundle unit 320 is rotated. Adjust the resolution due to the alignment direction.
  • the semi-tubular member 325 is attached to the IG bundle base 322 while maintaining the posture of the imaging unit 300 whose resolution has been adjusted, and the imaging unit 300 is inserted into the imaging hole 216 from the proximal end side of the distal end rigid member 211. insert. Accordingly, the imaging unit 300 can be positioned with respect to the distal end hard member 211 by abutting the distal end side end surface 325a of the semi-tubular member 325 against the abutting surface 217a of the imaging hole 216 while ensuring a desired resolution. .
  • FIG. 13 is a diagram showing a case where a prismatic member 326 is provided on the outer peripheral surface of the IG bundle base 322 as an abutting portion.
  • FIG. 14 is a diagram illustrating a case where a reverse concave member 327 is provided on the outer peripheral surface of the IG bundle base 322 as an abutting portion.
  • 327 may be provided separately from the IG bundle base 322 on the outer peripheral surface of the IG bundle base 322.
  • FIG. 15 is an enlarged view of the imaging unit 300 and the vicinity thereof in the distal end hard member 211 of the ultrasonic endoscope according to the second embodiment.
  • illustration of wiring connected to the ultrasonic transducer module 214 is omitted.
  • the groove 217 formed on the inner wall surface on the proximal end side of the imaging hole 216 in the distal end hard member 211 the groove 217 is formed on the inner wall surface on the treatment instrument insertion path 219 side.
  • the groove portion 217 may be formed in a semicircular shape on the inner wall surface on the side opposite to the treatment instrument insertion path 219 side.
  • a semi-tubular member 325 separate from the IG bundle base 322 is fixed to the outer peripheral surface of the IG bundle base 322 with an adhesive as the abutting portion that can pass through the semicircular groove 217.
  • the imaging unit 300 is inserted into the imaging hole 216 from the proximal end side of the distal end rigid member 211, and the distal end side end surface 325a of the semi-tubular member 325 is brought into contact with the abutting surface 217a of the imaging hole 216. And the imaging unit 300 is positioned with respect to the distal end hard member 211.
  • the wall thickness between the imaging hole 216 and the treatment instrument insertion passage 219 in the distal end hard member 211 is thicker than when the groove portion 217 is formed on the inner wall surface on the treatment instrument insertion passage 219 side. Therefore, the durability of the distal end hard member 211 can be increased accordingly. Further, since it is only necessary to secure a space between the abutting surface 217a and the semi-tubular member 325 on the proximal end side of the distal end hard member 211, imaging with respect to the distal end hard member 211 is performed while reducing the diameter of the distal end side of the distal end rigid member 211.
  • the unit 300 can be positioned.
  • the imaging unit 300 when assembling the imaging unit 300 to the distal end hard member 211, before the imaging unit 300 is inserted into the imaging hole 216, the imaging unit 300 is rotated about the axis, and each IG fiber of the IG bundle unit 320 is rotated. The resolution is adjusted due to the direction of alignment.
  • the semi-tubular member 325 is attached to the IG bundle base 322 while maintaining the posture of the imaging unit 300 whose resolution has been adjusted, and the imaging unit 300 is inserted into the imaging hole 216 from the proximal end side of the distal end rigid member 211. insert.
  • the imaging unit 300 can be positioned with respect to the distal end hard member 211 by abutting the distal end side end surface 325a of the semi-tubular member 325 against the abutting surface 217a of the imaging hole 216 while ensuring a desired resolution. .
  • the endoscope according to the present invention is useful for positioning the imaging unit with respect to the hard tip member while reducing the diameter of the hard tip member.

Abstract

This endoscope is equipped with: an imaging unit 300 which images a test subject and has a lens unit 310 and an image transmission unit; a rigid tip member 211 which is provided in the tip section of an insertion part 21 to be inserted into the test subject, and in which a treatment instrument insertion channel 219 is formed into which a treatment instrument for performing a prescribed treatment on the test subject is inserted, and an imaging hole 216 is formed in which the imaging unit 300 is positioned, wherein a groove section 217 is provided on the base side of the imaging hole 216; and an abutting section 314 which is provided inside the rigid tip member 211 on the base side of the imaging unit 300, and abuts the tip-side end surface of the groove section 217.

Description

内視鏡Endoscope
 本発明は、内視鏡に関する。 The present invention relates to an endoscope.
 従来、医療分野及び工業分野においては、各種検査のために内視鏡が広く用いられている。このうち、医療用の内視鏡は、患者等の被検体の体腔内に、撮像ユニットが設けられた挿入部を挿入することによって、被検体を切開しなくても体腔内の体内画像を取得できる。さらに、医療用の内視鏡は、挿入部の先端側から処置具を突出させて治療処置を行うことができる。これらの理由により、広く用いられている。 Conventionally, endoscopes have been widely used for various examinations in the medical field and the industrial field. Among these, medical endoscopes obtain in-vivo images in a body cavity without incising the subject by inserting an insertion unit provided with an imaging unit into the body cavity of the subject such as a patient. it can. Furthermore, the medical endoscope can perform a therapeutic treatment by protruding a treatment tool from the distal end side of the insertion portion. For these reasons, it is widely used.
 特許文献1に記載の内視鏡においては、挿入部の先端側に設けられた先端硬質部材内に、撮像ユニットを配設するための撮像用孔や、処置具用挿通路などが隣接して形成されている。先端硬質部材の先端面には、処置具用挿通路に挿入された処置具を被検体内に突出させるための処置具突出口が形成されている。また、撮像用孔に配置された撮像ユニットの撮像用レンズが、先端硬質部材の先端面から露出するように設けられている。 In the endoscope described in Patent Document 1, an imaging hole for disposing an imaging unit, a treatment instrument insertion passage, and the like are adjacent to each other in a distal end rigid member provided on the distal end side of the insertion portion. Is formed. On the distal end surface of the distal rigid member, a treatment instrument projecting port for projecting the treatment instrument inserted into the treatment instrument insertion path into the subject is formed. The imaging lens of the imaging unit disposed in the imaging hole is provided so as to be exposed from the distal end surface of the distal end hard member.
特開2005-261746号公報JP 2005-261746 A
 内視鏡の挿入部を組み立てる際には、撮像用孔の基端側から撮像ユニットを挿入し、撮像ユニットの先端側に設けられた突き当て部を、撮像用孔の先端側に設けられた突き当て面に突き当てることにより、先端硬質部材の先端面に対する撮像用レンズの位置が所定の位置となるように、先端硬質部材に対して撮像ユニットの位置決めがなされていた。しかしながら、撮像ユニットの先端側に前記突き当て面が設けられていると、先端硬質部材の先端側の細径化の妨げになるといった問題が生じ得る。 When assembling the insertion portion of the endoscope, the imaging unit is inserted from the proximal end side of the imaging hole, and the abutting portion provided on the distal end side of the imaging unit is provided on the distal end side of the imaging hole. The imaging unit is positioned with respect to the distal end hard member so that the position of the imaging lens with respect to the distal end surface of the distal end hard member becomes a predetermined position by being abutted against the abutting surface. However, when the abutting surface is provided on the distal end side of the imaging unit, there may arise a problem that the diameter of the distal end hard member is prevented from being reduced.
 本発明は、上記課題に鑑みてなされたものであって、その目的は、先端硬質部材の先端側の細径化を図りつつ、先端硬質部材に対する撮像ユニットの位置決めを行うことができる内視鏡を提供することである。 The present invention has been made in view of the above problems, and an object of the present invention is to provide an endoscope capable of positioning an imaging unit with respect to the distal end hard member while reducing the diameter of the distal end side of the distal end hard member. Is to provide.
 上述した課題を解決し、目的を達成するために、本発明に係る内視鏡は、レンズユニットと画像伝送ユニットとを有し、被検体を撮像する撮像ユニットと、前記被検体内に挿入される挿入部の先端部分に設けられ、該被検体に対して所定の処置を施す処置具が挿通される処置具用挿通路と、前記撮像ユニットが配設される撮像用孔とが形成され、該撮像用孔の基端側に溝部が設けられた先端硬質部材と、前記撮像ユニットの前記先端硬質部材内における基端側に設けられ、前記溝部の先端側端面と突き当たる突き当て部と、を備えることを特徴とするものである。 In order to solve the above-described problems and achieve the object, an endoscope according to the present invention has a lens unit and an image transmission unit, and is inserted into the subject, an imaging unit that images the subject. A treatment instrument insertion path through which a treatment instrument for performing a predetermined treatment on the subject is inserted, and an imaging hole in which the imaging unit is disposed, A distal end rigid member provided with a groove on the proximal end side of the imaging hole; and an abutting portion provided on the proximal end side in the distal end hard member of the imaging unit and abutting against the distal end side end surface of the groove. It is characterized by comprising.
 また、本発明に係る内視鏡は、上記の発明において、前記画像伝送ユニットは、画像伝送部材と、該画像伝送部材の先端側に設けられた口金とを有しており、前記口金とは別体で前記突き当て部を該口金の外周面に設けたことを特徴とするものである。 In the endoscope according to the present invention, in the above invention, the image transmission unit includes an image transmission member and a base provided on a distal end side of the image transmission member. The abutting portion is provided separately on the outer peripheral surface of the base.
 また、本発明に係る内視鏡は、上記の発明において、前記突き当て部はCリングであることを特徴とするものである。 The endoscope according to the present invention is characterized in that, in the above invention, the abutting portion is a C-ring.
 また、本発明に係る内視鏡は、上記の発明において、前記口金に対して前記Cリングが接着によって固定されていることを特徴とするものである。 Further, the endoscope according to the present invention is characterized in that, in the above invention, the C-ring is fixed to the base by adhesion.
 また、本発明に係る内視鏡は、上記の発明において、前記画像伝送部材は、複数のイメージガイドファイバが束ねられたイメージガイドバンドル、または、撮像素子と信号線とで構成されることを特徴とするものである。 In the endoscope according to the present invention as set forth in the invention described above, the image transmission member includes an image guide bundle in which a plurality of image guide fibers are bundled, or an imaging element and a signal line. It is what.
 また、本発明に係る内視鏡は、上記の発明において、前記先端硬質部材の前記撮像用孔と前記処置具用挿通路との間の肉厚が、該先端硬質部材の軸線方向で先端側から基端側にかけて変化しており、前記肉厚が最も薄い箇所よりも基端側に前記溝部の先端側端面が位置することを特徴とするものである。 Further, in the endoscope according to the present invention, in the above invention, the thickness between the imaging hole of the distal end hard member and the treatment instrument insertion path is the distal side in the axial direction of the distal end hard member. It changes from the base end side, The front end side end surface of the said groove part is located in the base end side rather than the location where the said thickness is the thinnest.
 本発明に係る内視鏡は、先端硬質部材の先端側の細径化を図りつつ、先端硬質部材に対する撮像ユニットの位置決めを行うことができるという効果を奏する。 The endoscope according to the present invention has an effect that the imaging unit can be positioned with respect to the hard tip member while reducing the diameter of the hard tip member.
図1は、実施の形態1に係る内視鏡システムを模式的に示す図である。FIG. 1 is a diagram schematically illustrating an endoscope system according to the first embodiment. 図2は、実施の形態1に係る超音波内視鏡の挿入部の先端構成を模式的に示す斜視図である。FIG. 2 is a perspective view schematically showing a distal end configuration of an insertion portion of the ultrasonic endoscope according to the first embodiment. 図3は、実施の形態1に係る超音波内視鏡の挿入部の先端構成を模式的に示す部分断面図である。FIG. 3 is a partial cross-sectional view schematically showing the distal end configuration of the insertion portion of the ultrasonic endoscope according to the first embodiment. 図4は、実施の形態1に係る撮像ユニットを示す斜視図である。FIG. 4 is a perspective view showing the imaging unit according to the first embodiment. 図5は、撮像ユニットに設けるCリングの斜視図である。FIG. 5 is a perspective view of a C-ring provided in the imaging unit. 図6は、IGバンドル口金にCリングを設けた状態におけるIGバンドル口金軸線方向から見た断面図である。FIG. 6 is a cross-sectional view of the IG bundle base as viewed from the axial direction of the IG bundle base in a state where the C ring is provided. 図7は、実施の形態1に係る超音波内視鏡の先端硬質部材内における撮像ユニット及びその近傍の拡大図である。FIG. 7 is an enlarged view of the imaging unit in the distal end hard member of the ultrasonic endoscope according to the first embodiment and the vicinity thereof. 図8は、比較例に係る超音波内視鏡の先端硬質部材内における撮像ユニット及びその近傍の拡大図である。FIG. 8 is an enlarged view of the imaging unit and the vicinity thereof in the distal end hard member of the ultrasonic endoscope according to the comparative example. 図9は、撮像ユニットの他例を示す斜視図である。FIG. 9 is a perspective view illustrating another example of the imaging unit. 図10は、撮像ユニットに設ける半管状部材の斜視図である。FIG. 10 is a perspective view of a semi-tubular member provided in the imaging unit. 図11は、IGバンドル口金に半管状部材を設けた状態におけるIGバンドル口金軸線方向から見た断面図である。FIG. 11 is a cross-sectional view seen from the axial direction of the IG bundle base in a state where the semi-tubular member is provided on the IG bundle base. 図12は、実施の形態1に係る超音波内視鏡の先端硬質部材内における撮像ユニット及びその近傍の他例の拡大図である。FIG. 12 is an enlarged view of another example of the imaging unit and its vicinity in the distal end hard member of the ultrasonic endoscope according to the first embodiment. 図13は、突き当て部として角柱形状部材を、IGバンドル口金の外周面に設けた場合を示す図である。FIG. 13 is a diagram illustrating a case where a prismatic member is provided as an abutting portion on the outer peripheral surface of the IG bundle base. 図14は、突き当て部として逆凹形状部材を、IGバンドル口金の外周面に設けた場合を示す図である。FIG. 14 is a diagram showing a case where an inverted concave member is provided as an abutting portion on the outer peripheral surface of the IG bundle base. 図15は、実施の形態2に係る超音波内視鏡の先端硬質部材内における撮像ユニット及びその近傍の拡大図である。FIG. 15 is an enlarged view of the imaging unit and the vicinity thereof in the distal end rigid member of the ultrasonic endoscope according to the second embodiment.
(実施の形態1)
 以下に、本発明を適用した内視鏡である超音波内視鏡の実施の形態1について、図面を参照して説明する。なお、以下に説明する実施の形態によって本発明が限定されるものではなく、例えば、超音波振動子を備えていない内視鏡においても本発明を適用することができる。さらに、図面の記載において、同一の部分には同一の符号を付している。
(Embodiment 1)
A first embodiment of an ultrasonic endoscope that is an endoscope to which the present invention is applied will be described below with reference to the drawings. Note that the present invention is not limited to the embodiments described below, and the present invention can be applied to, for example, an endoscope that does not include an ultrasonic transducer. Furthermore, the same code | symbol is attached | subjected to the same part in description of drawing.
 図1は、実施の形態1に係る超音波内視鏡2を備えた内視鏡システム1を模式的に示す図である。実施の形態1に係る内視鏡システム1は、図1に示すように、超音波内視鏡2と、超音波観測装置3と、内視鏡観察装置4と、表示装置5と、光源装置6とを備えており、超音波内視鏡2を用いて人等の被検体内の超音波診断を行うシステムである。 FIG. 1 is a diagram schematically showing an endoscope system 1 including an ultrasonic endoscope 2 according to the first embodiment. As shown in FIG. 1, an endoscope system 1 according to Embodiment 1 includes an ultrasonic endoscope 2, an ultrasonic observation device 3, an endoscope observation device 4, a display device 5, and a light source device. 6 is a system for performing ultrasonic diagnosis in a subject such as a person using the ultrasonic endoscope 2.
 超音波内視鏡2は、その先端部に設けられた超音波振動子によって、超音波観測装置3から受信した電気的なパルス信号を超音波パルス(音響パルス)に変換して被検体へ照射するとともに、被検体で反射された超音波エコーを電圧変化で表現する電気的なエコー信号に変換して出力する。 The ultrasonic endoscope 2 converts an electrical pulse signal received from the ultrasonic observation apparatus 3 into an ultrasonic pulse (acoustic pulse) and irradiates the subject with an ultrasonic transducer provided at the tip thereof. At the same time, the ultrasonic echo reflected from the subject is converted into an electrical echo signal expressed by a voltage change and output.
 超音波内視鏡2は、光学的に撮像を行う撮像ユニット300(図3参照)を有しており、被検体の消化管(食道、胃、十二指腸、大腸)、または呼吸器(気管、気管支)へ挿入され、消化管や呼吸器の撮像を行うことが可能である。また、その周囲臓器(膵臓、胆嚢、胆管、胆道、リンパ節、縦隔臓器、血管等)を、超音波を用いて撮像することが可能である。また、超音波内視鏡2は、撮像ユニット300による撮像時に被検体へ照射する照明光を導くライトガイドを有する。このライトガイドは、先端部が超音波内視鏡2の被検体への挿入部21の先端まで達している一方、基端部が照明光を発生する光源装置6に接続されている。 The ultrasound endoscope 2 includes an imaging unit 300 (see FIG. 3) that performs optical imaging, and the subject's digestive tract (esophagus, stomach, duodenum, large intestine), or respiratory organ (trachea, bronchus). It is possible to take images of the digestive tract and respiratory organs. In addition, surrounding organs (pancreas, gallbladder, bile duct, biliary tract, lymph node, mediastinal organ, blood vessel, etc.) can be imaged using ultrasound. In addition, the ultrasonic endoscope 2 has a light guide that guides illumination light to be irradiated onto the subject during imaging by the imaging unit 300. The light guide has a distal end portion reaching the distal end of the insertion portion 21 to the subject of the ultrasonic endoscope 2, and a proximal end portion connected to the light source device 6 that generates illumination light.
 また、超音波内視鏡2は、図1に示すように、挿入部21と、操作部22と、ユニバーサルコード23と、コネクタ24とを備える。挿入部21は、被検体内に挿入される部分である。この挿入部21は、図1に示すように、先端側に設けられ、超音波振動子7を保持する先端硬質部材211と、先端硬質部材211の基端側に連結され湾曲可能とする湾曲部212と、湾曲部212の基端側に連結され可撓性を有する可撓管部213とを備える。 Further, as shown in FIG. 1, the ultrasonic endoscope 2 includes an insertion portion 21, an operation portion 22, a universal cord 23, and a connector 24. The insertion part 21 is a part inserted into the subject. As shown in FIG. 1, the insertion portion 21 is provided on the distal end side, a distal end hard member 211 that holds the ultrasonic transducer 7, and a bending portion that is connected to the proximal end side of the distal end hard member 211 and can be bent. 212 and a flexible tube portion 213 connected to the proximal end side of the bending portion 212 and having flexibility.
 実施の形態1に係る内視鏡システム1においては、超音波振動子7として、複数の圧電素子をアレイ状に設け、送受信にかかわる圧電素子を電子的に切り替えたり、各圧電素子の送受信に遅延をかけたりすることによって、電子的に走査させるコンベックス型を採用している。なお、超音波振動子7の方式としては、コンベックス型に限るものではなく、ラジアル型やリニア型であってもよい。 In the endoscope system 1 according to the first embodiment, as the ultrasonic transducer 7, a plurality of piezoelectric elements are provided in an array, and the piezoelectric elements involved in transmission / reception are electronically switched, or the transmission / reception of each piezoelectric element is delayed. A convex type is employed in which scanning is performed electronically by applying the The method of the ultrasonic transducer 7 is not limited to the convex type, and may be a radial type or a linear type.
 ここで、挿入部21の内部には、具体的な図示は省略したが、光源装置6から供給された照明光を伝送するライトガイドや、各種信号を伝送する複数の信号ケーブルが引き回されているとともに、鉗子などの処置具を挿通するための処置具用挿通路219(図3参照)などが形成されている。 Here, although not shown in the drawings, a light guide that transmits illumination light supplied from the light source device 6 and a plurality of signal cables that transmit various signals are routed inside the insertion portion 21. In addition, a treatment instrument insertion passage 219 (see FIG. 3) for inserting a treatment instrument such as forceps is formed.
 操作部22は、挿入部21の基端側に連結され、医師等からの各種操作を受け付ける部分である。この操作部22は、図1に示すように、湾曲部212を湾曲操作するための湾曲ノブ221と、各種操作を行うための複数の操作部材222とを備える。また、操作部22には、処置具用挿通路219(図3参照)に連通し、処置具用挿通路219に処置具を挿通するための処置具挿入口223が形成されている。 The operation unit 22 is a part that is connected to the proximal end side of the insertion unit 21 and receives various operations from a doctor or the like. As shown in FIG. 1, the operation unit 22 includes a bending knob 221 for performing a bending operation on the bending unit 212 and a plurality of operation members 222 for performing various operations. In addition, the operation section 22 is formed with a treatment instrument insertion port 223 that communicates with the treatment instrument insertion path 219 (see FIG. 3) and allows the treatment instrument to be inserted into the treatment instrument insertion path 219.
 ユニバーサルコード23は、操作部22から延在し、各種信号を伝送する複数の信号ケーブル、及び、光源装置6から供給された照明光を伝送するライトガイド等が配設されたケーブルである。 The universal cord 23 is a cable that extends from the operation unit 22 and includes a plurality of signal cables that transmit various signals, a light guide that transmits illumination light supplied from the light source device 6, and the like.
 コネクタ24は、ユニバーサルコード23の先端に設けられており、超音波ケーブル31、ビデオケーブル41、及び、光源装置6がそれぞれ接続される第1コネクタ部241、第2コネクタ部242、及び、第3コネクタ部243を備える。 The connector 24 is provided at the tip of the universal cord 23, and the first connector part 241, the second connector part 242, and the third connector to which the ultrasonic cable 31, the video cable 41, and the light source device 6 are connected, respectively. A connector portion 243 is provided.
 超音波観測装置3は、超音波ケーブル31を介して超音波内視鏡2に電気的に接続しており、超音波ケーブル31を介して超音波内視鏡2にパルス信号を出力するとともに超音波内視鏡2からエコー信号が入力される。そして、超音波観測装置3は、前記エコー信号に所定の処理を施して超音波画像を生成する。 The ultrasonic observation apparatus 3 is electrically connected to the ultrasonic endoscope 2 via the ultrasonic cable 31 and outputs a pulse signal to the ultrasonic endoscope 2 via the ultrasonic cable 31 and is supersonic. An echo signal is input from the sonic endoscope 2. Then, the ultrasonic observation device 3 performs a predetermined process on the echo signal to generate an ultrasonic image.
 内視鏡観察装置4は、ビデオケーブル41を介して超音波内視鏡2に電気的に接続しており、ビデオケーブル41を介して超音波内視鏡2からの画像信号が入力される。そして、内視鏡観察装置4は、前記画像信号に所定の処理を施して内視鏡画像を生成する。 The endoscope observation apparatus 4 is electrically connected to the ultrasonic endoscope 2 via a video cable 41, and an image signal from the ultrasonic endoscope 2 is input via the video cable 41. Then, the endoscope observation apparatus 4 performs a predetermined process on the image signal to generate an endoscope image.
 表示装置5は、液晶または有機EL(Electro Luminescence)、プロジェクタ、CRT(Cathode Ray Tube)などを用いて構成されており、超音波観測装置3にて生成された超音波画像や、内視鏡観察装置4にて生成された内視鏡画像等を表示する。 The display device 5 is configured by using a liquid crystal or organic EL (Electro Luminescence), a projector, a CRT (Cathode Ray Tube), etc., and an ultrasonic image generated by the ultrasonic observation device 3 or an endoscope observation. An endoscopic image generated by the apparatus 4 is displayed.
 光源装置6は、被検体内を照明する照明光を超音波内視鏡2に供給する。 The light source device 6 supplies illumination light for illuminating the inside of the subject to the ultrasonic endoscope 2.
 図2は、実施の形態1に係る超音波内視鏡2の挿入部21の先端構成を示す斜視図である。図3は、実施の形態1に係る超音波内視鏡2の挿入部21の先端構成を示す部分断面図である。なお、図3においては、超音波振動子モジュール214に接続される配線の図示は省略している。図2及び図3に示すように、挿入部21の先端側は、超音波振動子7を保持する超音波振動子モジュール214と、内視鏡モジュール215とで構成されている。また、内視鏡モジュール215の先端側傾斜面には、照明ユニットを構成する照明用レンズ215a、撮像ユニット300を構成する観察窓215b、及び、鉗子などの処置具を突出させるための処置具突出口215cが設けられている。 FIG. 2 is a perspective view showing a distal end configuration of the insertion portion 21 of the ultrasonic endoscope 2 according to the first embodiment. FIG. 3 is a partial cross-sectional view showing the distal end configuration of the insertion portion 21 of the ultrasonic endoscope 2 according to the first embodiment. In FIG. 3, illustration of wiring connected to the ultrasonic transducer module 214 is omitted. As shown in FIGS. 2 and 3, the distal end side of the insertion portion 21 includes an ultrasonic transducer module 214 that holds the ultrasonic transducer 7 and an endoscope module 215. Further, on the tip side inclined surface of the endoscope module 215, an illumination lens 215a constituting the illumination unit, an observation window 215b constituting the imaging unit 300, and a treatment tool protrusion for projecting a treatment tool such as forceps are projected. A mouth 215c is provided.
 内視鏡モジュール215の先端硬質部材211内には、撮像ユニット300を配設するための撮像用孔216が、挿入部21の長手軸方向に対して傾斜して設けられている。また、先端硬質部材211内には、処置具突出口215cと連通する処置具用挿通路219が設けられており、処置具用挿通路219の処置具突出口215cに連なる端部近傍が、先端硬質部材211の軸線方向に対して上方に傾斜しており、処置具が処置具突出口215cから前記軸線方向に対して上方に傾斜した方向に突出するように設けられている。 In the distal end hard member 211 of the endoscope module 215, an imaging hole 216 for arranging the imaging unit 300 is provided to be inclined with respect to the longitudinal axis direction of the insertion portion 21. Further, a treatment instrument insertion passage 219 communicating with the treatment instrument protrusion 215c is provided in the distal end hard member 211, and the vicinity of the end portion of the treatment instrument insertion passage 219 connected to the treatment instrument protrusion 215c is the distal end. It is inclined upward with respect to the axial direction of the hard member 211, and the treatment instrument is provided so as to protrude in a direction inclined upward with respect to the axial direction from the treatment instrument protrusion 215c.
 なお、ここで言う先端硬質部材211の軸線方向とは、挿入部21を真っ直ぐに伸ばした際の長手方向に沿った方向である。また、先端硬質部材211の軸線方向に対して上方とは、撮像ユニット300に対して処置具用挿通路219が上に位置しており、撮像ユニット300に対して超音波振動子モジュール214が下に位置する、図2及び図3に示すような姿勢をとっている内視鏡モジュール215におけるものである。 In addition, the axial direction of the distal end hard member 211 referred to here is a direction along the longitudinal direction when the insertion portion 21 is straightened. Further, “above the distal end rigid member 211 in the axial direction” means that the treatment instrument insertion path 219 is located above the imaging unit 300 and the ultrasonic transducer module 214 is located below the imaging unit 300. The endoscope module 215 is located at the position shown in FIGS. 2 and 3.
 撮像ユニット300は、レンズユニット310と、画像伝送ユニットであるイメージガイドバンドルユニット(以下、IGバンドルユニットという)320とで構成されている。なお、画像伝送ユニットとしては、CCD(Charge Coupled Device)やCMOS(Complementary Metal Oxide Semiconductor)などの撮像素子と信号線とで構成されたものであってもよい。 The imaging unit 300 includes a lens unit 310 and an image guide bundle unit (hereinafter referred to as an IG bundle unit) 320 that is an image transmission unit. The image transmission unit may be configured by an image sensor such as a CCD (Charge Coupled Device) or CMOS (Complementary Metal Oxide Semiconductor) and a signal line.
 レンズユニット310は、観察窓215bや対物レンズ311,312などの複数のレンズが筒状部材であるレンズ枠313に保持されて構成されており、対物レンズ312の基端側の面には、イメージガイドファイバ(以下、IGファイバという)の先端が突き当てられている。また、レンズ枠313の基端側は、IGバンドル口金322の先端側と接着剤で固定されている。 The lens unit 310 is configured by holding a plurality of lenses such as an observation window 215b and objective lenses 311 and 312 in a lens frame 313 that is a cylindrical member. The tip of a guide fiber (hereinafter referred to as IG fiber) is abutted. Further, the proximal end side of the lens frame 313 is fixed to the distal end side of the IG bundle base 322 with an adhesive.
 IGバンドルユニット320は、湾曲部212及び可撓管部213内を通って操作部22まで導かれている複数のIGファイバを束ねたイメージガイドバンドル(以下、IGバンドルという)321と、このIGバンドル321の先端側を内包する筒状部材であるIGバンドル口金322と、IGバンドル321のIGバンドル口金322よりも基端側を内包する軟性チューブ323とを備えている。 The IG bundle unit 320 includes an image guide bundle (hereinafter referred to as an IG bundle) 321 in which a plurality of IG fibers guided to the operation unit 22 through the bending portion 212 and the flexible tube portion 213, and the IG bundle. An IG bundle base 322 which is a cylindrical member including the distal end side of the 321 and a flexible tube 323 including a base end side of the IG bundle base 322 of the IG bundle 321 are provided.
 図4は、実施の形態1に係る撮像ユニット300を示す斜視図である。図5は、撮像ユニット300に設けるCリング324の斜視図である。図6は、IGバンドル口金322にCリング324を設けた状態におけるIGバンドル口金軸線方向から見た断面図である。 FIG. 4 is a perspective view showing the imaging unit 300 according to the first embodiment. FIG. 5 is a perspective view of the C ring 324 provided in the imaging unit 300. FIG. 6 is a cross-sectional view seen from the axis direction of the IG bundle base when the C ring 324 is provided on the IG bundle base 322.
 実施の形態1に係る超音波内視鏡2においては、先端硬質部材211に対する撮像ユニット300の位置決め用の突き当て部として、図5に示すようなCリング324を、撮像ユニット300の先端硬質部材211内における基端側、具体的には、図4及び図6に示すようにIGバンドル口金322の外周面に、IGバンドル口金322とは別体で設けている。このCリング324は、接着剤によってIGバンドル口金322の外周面に固定されている。なお、Cリング324は、ステンレス鋼、チタン、チタン合金、及び、Cu-Zn系合金(真鍮)などの金属によって構成されている。そして、IGバンドル口金322とCリング324とが金属で構成されている場合には、接着剤ではなく溶接によって、Cリング324をIGバンドル口金322の外周面に固定しても良い。また、前記突き当て部としては、IGバンドル口金322と一体で、IGバンドル口金322の外周面に設けても良い。 In the ultrasonic endoscope 2 according to the first embodiment, a C ring 324 as shown in FIG. 5 is used as the abutting portion for positioning the imaging unit 300 with respect to the distal end hard member 211, and the distal end rigid member of the imaging unit 300. The base end side in 211, specifically, as shown in FIGS. 4 and 6, is provided on the outer peripheral surface of the IG bundle base 322 separately from the IG bundle base 322. The C ring 324 is fixed to the outer peripheral surface of the IG bundle base 322 with an adhesive. The C ring 324 is made of a metal such as stainless steel, titanium, a titanium alloy, and a Cu—Zn alloy (brass). When the IG bundle base 322 and the C ring 324 are made of metal, the C ring 324 may be fixed to the outer peripheral surface of the IG bundle base 322 by welding instead of an adhesive. Further, the abutting portion may be provided integrally with the IG bundle base 322 and provided on the outer peripheral surface of the IG bundle base 322.
 図7は、実施の形態1に係る超音波内視鏡2の先端硬質部材211内における撮像ユニット300及びその近傍の拡大図である。なお、図7においては、超音波振動子モジュール214に接続される配線の図示は省略している。図7に示すように、撮像用孔216の基端側における内壁面には、IGバンドル口金322の外周面に設けられたCリング324が突き当たる段差が形成されている。この段差は、IGバンドル口金322に設けられたCリング324が通過可能な溝部217を、撮像用孔216の基端側における内壁面に撮像用孔216の軸線方向に沿って設けることによって形成される。この溝部217の基端側端面は開放しており、溝部217の先端側端面が前記段差を構成する、Cリング324の先端側端面324aと突き当たる突き当て面217aとなっている。そして、この溝部217に設けられた突き当て面217aと、IGバンドル口金322に設けられたCリング324の先端側端面324aとを突き当てることによって、先端硬質部材211に対する撮像ユニット300の位置決めがなされる。 FIG. 7 is an enlarged view of the imaging unit 300 and its vicinity in the distal end hard member 211 of the ultrasonic endoscope 2 according to the first embodiment. In FIG. 7, illustration of wiring connected to the ultrasonic transducer module 214 is omitted. As shown in FIG. 7, a step where the C ring 324 provided on the outer peripheral surface of the IG bundle base 322 abuts is formed on the inner wall surface on the proximal end side of the imaging hole 216. This step is formed by providing a groove 217 through which the C-ring 324 provided in the IG bundle base 322 can pass along the axial direction of the imaging hole 216 on the inner wall surface on the proximal end side of the imaging hole 216. The The base end side end surface of the groove portion 217 is open, and the front end side end surface of the groove portion 217 forms an abutting surface 217 a that abuts against the front end side end surface 324 a of the C ring 324. Then, the imaging unit 300 is positioned with respect to the distal end hard member 211 by abutting the abutting surface 217a provided in the groove 217 and the distal end side end surface 324a of the C ring 324 provided in the IG bundle base 322. The
 なお、実施の形態1における先端硬質部材211に対する撮像ユニット300の位置決めとは、撮像ユニット300のレンズユニット310に設けられた観察窓215bが、先端硬質部材211の先端側傾斜面に対して、撮像用孔216の先端側開口から出過ぎたり入り込み過ぎたりしない所定の位置に位置するように、撮像ユニット300を先端硬質部材211に組み付けることである。 The positioning of the imaging unit 300 with respect to the distal end hard member 211 in the first embodiment refers to the imaging of the observation window 215b provided in the lens unit 310 of the imaging unit 300 with respect to the distal end inclined surface of the distal end hard member 211. That is, the imaging unit 300 is assembled to the distal end hard member 211 so as to be located at a predetermined position where it does not go out or enter too much from the opening on the distal end side of the hole 216.
 ここで、先端硬質部材211内における処置具用挿通路219の途中には、処置具用挿通路219を屈曲させる屈曲部219aが設けられており、撮像用孔216に対して処置具用挿通路219が、基端側から屈曲部219a側に向かうにしたがって撮像用孔216に近づくように傾斜し、屈曲部219aから先端側(処置具突出口215c側)に向かうにしたがって撮像用孔216から遠ざかるように傾斜している。これにより、先端硬質部材211の撮像用孔216と処置具用挿通路219との間の肉厚は、先端側から基端側にかけて変化しており、屈曲部219aが位置する部分において前記肉厚が最も薄くなる。 Here, in the middle of the treatment instrument insertion path 219 in the distal end hard member 211, a bending portion 219 a for bending the treatment instrument insertion path 219 is provided, and the treatment instrument insertion path with respect to the imaging hole 216 is provided. 219 is inclined so as to approach the imaging hole 216 from the base end side toward the bent portion 219a side, and away from the imaging hole 216 from the bent portion 219a toward the distal end side (the treatment instrument protrusion port 215c side). So as to be inclined. Thereby, the thickness between the imaging hole 216 of the distal end rigid member 211 and the treatment instrument insertion path 219 changes from the distal end side to the proximal end side, and the thickness is increased at the portion where the bent portion 219a is located. Becomes the thinnest.
 そして、実施の形態1においては、先端硬質部材211内における前記肉厚が最も薄い箇所(屈曲部219aが位置する部分)よりも基端側に、突き当て面217aが位置するように溝部217を設けるとともに、突き当て面217aの位置に対応させてCリング324をIGバンドル口金322の外周面に設けている。 In the first embodiment, the groove portion 217 is formed so that the abutting surface 217a is positioned closer to the base end side than the thinnest portion (the portion where the bent portion 219a is located) in the distal end hard member 211. At the same time, a C ring 324 is provided on the outer peripheral surface of the IG bundle base 322 in correspondence with the position of the abutting surface 217a.
 図8は、比較例に係る超音波内視鏡2の先端硬質部材211内における撮像ユニット300及びその近傍の拡大図である。なお、図8においては、超音波振動子モジュール214に接続される配線の図示は省略している。図8に示すように比較例においては、撮像ユニット300の先端硬質部材211内における先端側、具体的には、レンズ枠313に、突き当て部314がレンズ枠313と一体で設けられている。また、先端硬質部材211の基端側から撮像用孔216内に撮像ユニット300を挿入した際、レンズ枠313に設けられた突き当て部314が通過可能な溝部218が、撮像用孔216の内壁面に基端側から先端側にかけて設けられている。そして、この溝部218の先端側端面である突き当て面218aと、レンズ枠313に設けられた突き当て部314の先端側端面314aとを突き当てることによって、先端硬質部材211に対する撮像ユニット300の位置決めがなされる。 FIG. 8 is an enlarged view of the imaging unit 300 and its vicinity in the distal end hard member 211 of the ultrasonic endoscope 2 according to the comparative example. In FIG. 8, illustration of wiring connected to the ultrasonic transducer module 214 is omitted. As shown in FIG. 8, in the comparative example, the abutting portion 314 is provided integrally with the lens frame 313 on the distal end side in the distal end hard member 211 of the imaging unit 300, specifically, on the lens frame 313. Further, when the imaging unit 300 is inserted into the imaging hole 216 from the proximal end side of the distal end hard member 211, a groove 218 through which the abutting part 314 provided in the lens frame 313 can pass is formed in the imaging hole 216. It is provided in the wall surface from the base end side to the front end side. Then, the imaging unit 300 is positioned with respect to the distal end hard member 211 by abutting the abutting surface 218a which is the distal end side end surface of the groove portion 218 and the distal end side end surface 314a of the abutting portion 314 provided on the lens frame 313. Is made.
 そのため、比較例においては、前記肉厚が最も薄い箇所(屈曲部219aが位置する部分)にも溝部218が延在しているため、前記最も薄い箇所における前記肉厚が、溝部218の深さ分だけさらに薄くなり、その結果、先端硬質部材211の耐久性が低下してしまう。また、先端硬質部材211の先端側に突き当て面218aや突き当て部314のためのスペースを確保する必要があり、先端硬質部材211の先端側の細径化の妨げになってしまう。 Therefore, in the comparative example, since the groove portion 218 extends also in the thinnest portion (the portion where the bent portion 219a is located), the thickness in the thinnest portion is the depth of the groove portion 218. As a result, the durability of the distal end hard member 211 is reduced. In addition, it is necessary to secure a space for the abutting surface 218 a and the abutting portion 314 on the distal end side of the distal end hard member 211, which hinders a reduction in diameter on the distal end side of the distal end hard member 211.
 これに対して、実施の形態1に係る超音波内視鏡2においては、前記肉厚が最も薄い箇所(処置具用挿通路219の屈曲部219aが位置する部分)まで溝部217が延在していないため、前記肉厚が薄くなり過ぎて、先端硬質部材211の耐久性が低下してしまうのを抑制することができる。また、先端硬質部材211の基端側に突き当て面217a及びCリング324のスペースを確保すれば良いため、先端硬質部材211の先端側の細径化を図りつつ、先端硬質部材211に対する撮像ユニット300の位置決めを行うことができる。 In contrast, in the ultrasonic endoscope 2 according to the first embodiment, the groove portion 217 extends to the thinnest portion (the portion where the bent portion 219a of the treatment instrument insertion path 219 is located). Therefore, it can be suppressed that the thickness of the tip hard member 211 is deteriorated because the thickness is too thin. In addition, since it is only necessary to secure a space between the abutting surface 217a and the C ring 324 on the proximal end side of the distal end hard member 211, an imaging unit for the distal end hard member 211 while reducing the diameter on the distal end side of the distal end hard member 211 300 positionings can be performed.
 また、実施の形態1に係る超音波内視鏡2においては、撮像用孔216の基端側における内壁面の円周方向でほぼ全周にわたって溝部217が形成されている。実施の形態1では、先端硬質部材211に撮像ユニット300を組み付ける際、IGバンドルユニット320の各IGファイバの並び方向に起因した解像度の調整のために、撮像用孔216内で撮像ユニット300を回転させる。そのため、撮像用孔216の基端側における内壁面の円周方向でほぼ全周にわたって溝部217が形成されていることにより、前記内壁面の円周方向でほぼ全周にわたって突き当て面217aが設けられるため、所望の解像度に調整された後に撮像ユニット300の回転に伴ってCリング324がどの向きを向いていても、突き当て面217aにCリング324の先端側端面324aを確実に突き当てて、先端硬質部材211に対する撮像ユニット300の位置決めを行うことができる。 Further, in the ultrasonic endoscope 2 according to the first embodiment, the groove portion 217 is formed over the entire circumference in the circumferential direction of the inner wall surface on the proximal end side of the imaging hole 216. In the first embodiment, when the imaging unit 300 is assembled to the distal end hard member 211, the imaging unit 300 is rotated in the imaging hole 216 in order to adjust the resolution due to the arrangement direction of the IG fibers of the IG bundle unit 320. Let Therefore, the groove portion 217 is formed over the entire circumference in the circumferential direction of the inner wall surface on the proximal end side of the imaging hole 216, so that the abutting surface 217a is provided over the entire circumference in the circumferential direction of the inner wall surface. Therefore, even if the C ring 324 faces in any direction as the imaging unit 300 rotates after the adjustment to the desired resolution, the end surface 324a on the front end side of the C ring 324 is reliably abutted against the abutting surface 217a. The imaging unit 300 can be positioned with respect to the distal end hard member 211.
 次に、撮像ユニット300の組み立てについて説明する。実施の形態1においては、まず、レンズ枠313の先端側端部に観察窓215bと対物レンズ311とを配設する。次に、IGバンドル口金322の先端側開口と、IGバンドル321を構成するIGファイバの先端とが面一となるように、IGバンドル口金322内にIGバンドル321を配設し、IGバンドル口金322とIGバンドル321とを接着剤などで固定する。なお、IGバンドル321には、先端側のIGバンドル口金322が設けられる部分を除いて予め軟性チューブ323が設けられている。次に、レンズユニット310を構成する対物レンズ312の基端側の面と、IGバンドル口金322内に配設されたIGファイバの先端とを接触させて、対物レンズ312をIGバンドル口金322の先端側端面に接着剤などによって固定する。そして、このように対物レンズ312が固定されたIGバンドルユニット320の先端部分を、レンズ枠313の基端側開口からレンズ枠313内に挿入する。そして、レンズ枠313内でIGバンドルユニット320を進退させて、対物レンズ311と対物レンズ312との間の距離を調整し、ピント調整などの光学調整を行った後、レンズ枠313に対してIGバンドル口金322を接着剤などによって接着して固定する。これにより、レンズユニット310とIGバンドルユニット320とが一体となって撮像ユニット300の組み立てが完了する。 Next, assembly of the imaging unit 300 will be described. In the first embodiment, first, the observation window 215b and the objective lens 311 are disposed at the end of the lens frame 313 on the front end side. Next, the IG bundle 321 is disposed in the IG bundle base 322 so that the opening on the front end side of the IG bundle base 322 and the front end of the IG fiber constituting the IG bundle 321 are flush with each other. And the IG bundle 321 are fixed with an adhesive or the like. The IG bundle 321 is provided with a flexible tube 323 in advance, except for a portion where the tip side IG bundle base 322 is provided. Next, the surface of the base end side of the objective lens 312 constituting the lens unit 310 and the tip of the IG fiber disposed in the IG bundle base 322 are brought into contact with each other, so that the objective lens 312 is brought into contact with the tip of the IG bundle base 322. Fix to the side edge with adhesive. Then, the distal end portion of the IG bundle unit 320 to which the objective lens 312 is fixed in this manner is inserted into the lens frame 313 from the proximal end side opening of the lens frame 313. Then, the IG bundle unit 320 is moved back and forth in the lens frame 313 to adjust the distance between the objective lens 311 and the objective lens 312, and after performing optical adjustment such as focus adjustment, the IG bundle unit 320 is moved toward the lens frame 313. The bundle base 322 is bonded and fixed with an adhesive or the like. Thereby, the lens unit 310 and the IG bundle unit 320 are integrated, and the assembly of the imaging unit 300 is completed.
 また、このように撮像ユニット300を組み立てた後、レンズユニット310の先端から所定距離だけ離して、IGバンドル口金322の外周面にCリング324を接着剤などで固定して設ける。そして、先端硬質部材211の基端側から撮像用孔216内に撮像ユニット300を挿入し、撮像用孔216の基端側における内壁面に形成された溝部217を通して突き当て面217aにCリング324の先端側端面324aを突き当てて、先端硬質部材211に対する撮像ユニット300の位置決めを行う。 In addition, after assembling the imaging unit 300 in this way, the C ring 324 is fixed to the outer peripheral surface of the IG bundle base 322 with an adhesive or the like at a predetermined distance from the tip of the lens unit 310. Then, the imaging unit 300 is inserted into the imaging hole 216 from the base end side of the distal end hard member 211, and the C ring 324 is formed on the abutting surface 217a through the groove portion 217 formed on the inner wall surface on the base end side of the imaging hole 216. The imaging unit 300 is positioned with respect to the distal end hard member 211 by abutting against the distal end side end surface 324a.
 このように、先端硬質部材211に対する撮像ユニット300の位置決めを行った後、IGバンドルユニット320の各IGファイバの並び方向に起因した解像度の調整のために、撮像用孔216内で撮像ユニット300を回転させる。そして、解像度の調整を行った後、撮像ユニット300を接着剤などによって先端硬質部材211に固定することにより、先端硬質部材211への撮像ユニット300の組み付けが完了する。 Thus, after positioning the imaging unit 300 with respect to the distal end hard member 211, the imaging unit 300 is placed in the imaging hole 216 in order to adjust the resolution caused by the arrangement direction of the IG fibers of the IG bundle unit 320. Rotate. Then, after the resolution is adjusted, the imaging unit 300 is fixed to the distal end hard member 211 with an adhesive or the like, whereby the assembly of the imaging unit 300 to the distal end hard member 211 is completed.
 図9は、撮像ユニット300の他例を示す斜視図である。図10は、撮像ユニット300に設ける半管状部材325の斜視図である。図11は、IGバンドル口金322に半管状部材325を設けた状態におけるIGバンドル口金軸線方向から見た断面図である。図12は、実施の形態1に係る超音波内視鏡2の先端硬質部材211内における撮像ユニット300及びその近傍の他例の拡大図である。なお、図12においては、超音波振動子モジュール214に接続される配線の図示は省略している。 FIG. 9 is a perspective view showing another example of the imaging unit 300. FIG. 10 is a perspective view of the semi-tubular member 325 provided in the imaging unit 300. FIG. 11 is a cross-sectional view as viewed from the axial direction of the IG bundle base in a state where the semi-tubular member 325 is provided on the IG bundle base 322. FIG. 12 is an enlarged view of another example of the imaging unit 300 and the vicinity thereof in the distal end hard member 211 of the ultrasonic endoscope 2 according to the first embodiment. In FIG. 12, illustration of wiring connected to the ultrasonic transducer module 214 is omitted.
 図9に示す撮像ユニット300においては、IGバンドル口金322に設ける前記突き当て部として、Cリング324に替えて、図10に示すような半管状部材325を用いている。半管状部材325は、図11に示すように、IGバンドル口金322の外周面にIGバンドル口金322とは別体で設けられており、IGバンドル口金322と半管状部材325とが接着剤によって固定されている。そして、図12に示すように、半管状部材325の先端側端面325aを撮像用孔216の突き当て面217aに突き当てて、先端硬質部材211に対する撮像ユニット300の位置決めを行う。 In the imaging unit 300 shown in FIG. 9, a semi-tubular member 325 as shown in FIG. 10 is used instead of the C ring 324 as the abutting portion provided in the IG bundle base 322. As shown in FIG. 11, the semi-tubular member 325 is provided separately from the IG bundle base 322 on the outer peripheral surface of the IG bundle base 322, and the IG bundle base 322 and the semi-tubular member 325 are fixed by an adhesive. Has been. Then, as shown in FIG. 12, the front end side end surface 325 a of the semi-tubular member 325 is abutted against the abutting surface 217 a of the imaging hole 216, and the imaging unit 300 is positioned with respect to the distal end hard member 211.
 なお、撮像ユニット300の前記突き当て部として、IGバンドル口金322に半管状部材325を設けた場合には、撮像用孔216の基端側における内壁面の円周方向でほぼ全周にわたって溝部217を形成しても良いし、前記内壁面の円周方向で処置具用挿通路219側にだけ半円形状で溝部217を形成してもよい。一方、半円形状の溝部217を形成した場合には、撮像用孔216内に撮像ユニット300を挿入する前に、撮像ユニット300を軸線中心で回転させて、IGバンドルユニット320の各IGファイバの並び方向に起因した解像度の調整を行う。そして、解像度の調整が終わった撮像ユニット300の姿勢を保ったまま、IGバンドル口金322に半管状部材325を取り付けて、先端硬質部材211の基端側から撮像用孔216内に撮像ユニット300を挿入する。これにより、所望の解像度を確保しつつ、半管状部材325の先端側端面325aを撮像用孔216の突き当て面217aに突き当てて、先端硬質部材211に対する撮像ユニット300の位置決めを行うことができる。 When the semi-tubular member 325 is provided in the IG bundle base 322 as the abutting portion of the imaging unit 300, the groove portion 217 extends substantially over the entire circumference in the circumferential direction of the inner wall surface on the proximal end side of the imaging hole 216. Alternatively, the groove 217 may be formed in a semicircular shape only on the treatment instrument insertion passage 219 side in the circumferential direction of the inner wall surface. On the other hand, when the semicircular groove 217 is formed, before the imaging unit 300 is inserted into the imaging hole 216, the imaging unit 300 is rotated about the axis, and each IG fiber of the IG bundle unit 320 is rotated. Adjust the resolution due to the alignment direction. The semi-tubular member 325 is attached to the IG bundle base 322 while maintaining the posture of the imaging unit 300 whose resolution has been adjusted, and the imaging unit 300 is inserted into the imaging hole 216 from the proximal end side of the distal end rigid member 211. insert. Accordingly, the imaging unit 300 can be positioned with respect to the distal end hard member 211 by abutting the distal end side end surface 325a of the semi-tubular member 325 against the abutting surface 217a of the imaging hole 216 while ensuring a desired resolution. .
 図13は、突き当て部として角柱形状部材326を、IGバンドル口金322の外周面に設けた場合を示す図である。図14は、突き当て部として逆凹形状部材327を、IGバンドル口金322の外周面に設けた場合を示す図である。撮像ユニット300の基端側に設ける前記突き当て部としては、図13に示すような角柱形状部材326や、図14に示すようなIGバンドル口金322の外周面と接する側が凹んだ逆凹形状部材327などを、IGバンドル口金322の外周面にIGバンドル口金322と別体で設けて構成してもよい。 FIG. 13 is a diagram showing a case where a prismatic member 326 is provided on the outer peripheral surface of the IG bundle base 322 as an abutting portion. FIG. 14 is a diagram illustrating a case where a reverse concave member 327 is provided on the outer peripheral surface of the IG bundle base 322 as an abutting portion. As the abutting portion provided on the base end side of the imaging unit 300, a prismatic member 326 as shown in FIG. 13 or a reverse concave member whose side contacting the outer peripheral surface of the IG bundle base 322 as shown in FIG. 14 is recessed. 327 may be provided separately from the IG bundle base 322 on the outer peripheral surface of the IG bundle base 322.
(実施の形態2)
 以下に、本発明を適用した内視鏡の実施の形態2について、図面を参照して説明する。なお、図面の記載において、上記実施の形態1と同一の部分には同一の符号を付している。
(Embodiment 2)
Embodiment 2 of an endoscope to which the present invention is applied will be described below with reference to the drawings. In the description of the drawings, the same parts as those in the first embodiment are denoted by the same reference numerals.
 図15は、実施の形態2に係る超音波内視鏡の先端硬質部材211内における撮像ユニット300及びその近傍の拡大図である。なお、図15においては、超音波振動子モジュール214に接続される配線の図示は省略している。図15に示すように、先端硬質部材211内における撮像用孔216の基端側における内壁面に形成する溝部217としては、処置具用挿通路219側にある前記内壁面には溝部217を形成せず、処置具用挿通路219側とは反対側にある前記内壁面に半円形状で溝部217を形成してもよい。また、この場合には、半円形状の溝部217を通過可能な前記突き当て部として、IGバンドル口金322とは別体の半管状部材325を接着剤によってIGバンドル口金322の外周面に固定して設ける。そして、図15に示すように、先端硬質部材211の基端側から撮像用孔216内に撮像ユニット300を挿入し、撮像用孔216の突き当て面217aに半管状部材325の先端側端面325aを突き当てて、先端硬質部材211に対する撮像ユニット300の位置決めを行う。 FIG. 15 is an enlarged view of the imaging unit 300 and the vicinity thereof in the distal end hard member 211 of the ultrasonic endoscope according to the second embodiment. In FIG. 15, illustration of wiring connected to the ultrasonic transducer module 214 is omitted. As shown in FIG. 15, as the groove 217 formed on the inner wall surface on the proximal end side of the imaging hole 216 in the distal end hard member 211, the groove 217 is formed on the inner wall surface on the treatment instrument insertion path 219 side. Instead, the groove portion 217 may be formed in a semicircular shape on the inner wall surface on the side opposite to the treatment instrument insertion path 219 side. In this case, a semi-tubular member 325 separate from the IG bundle base 322 is fixed to the outer peripheral surface of the IG bundle base 322 with an adhesive as the abutting portion that can pass through the semicircular groove 217. Provide. Then, as shown in FIG. 15, the imaging unit 300 is inserted into the imaging hole 216 from the proximal end side of the distal end rigid member 211, and the distal end side end surface 325a of the semi-tubular member 325 is brought into contact with the abutting surface 217a of the imaging hole 216. And the imaging unit 300 is positioned with respect to the distal end hard member 211.
 これにより、処置具用挿通路219側にある前記内壁面に溝部217を形成した場合よりも、先端硬質部材211内における撮像用孔216と処置具用挿通路219との間の肉厚を厚くすることができ、その分、先端硬質部材211の耐久性を高めることができる。また、先端硬質部材211の基端側に突き当て面217a及び半管状部材325のスペースを確保すれば良いため、先端硬質部材211の先端側の細径化を図りつつ、先端硬質部材211に対する撮像ユニット300の位置決めを行うことができる。 Accordingly, the wall thickness between the imaging hole 216 and the treatment instrument insertion passage 219 in the distal end hard member 211 is thicker than when the groove portion 217 is formed on the inner wall surface on the treatment instrument insertion passage 219 side. Therefore, the durability of the distal end hard member 211 can be increased accordingly. Further, since it is only necessary to secure a space between the abutting surface 217a and the semi-tubular member 325 on the proximal end side of the distal end hard member 211, imaging with respect to the distal end hard member 211 is performed while reducing the diameter of the distal end side of the distal end rigid member 211. The unit 300 can be positioned.
 また、先端硬質部材211に撮像ユニット300を組み付ける際には、撮像用孔216内に撮像ユニット300を挿入する前に、撮像ユニット300を軸線中心で回転させて、IGバンドルユニット320の各IGファイバの並び方向に起因した解像度の調整を行う。そして、解像度の調整が終わった撮像ユニット300の姿勢を保ったまま、IGバンドル口金322に半管状部材325を取り付けて、先端硬質部材211の基端側から撮像用孔216内に撮像ユニット300を挿入する。これにより、所望の解像度を確保しつつ、半管状部材325の先端側端面325aを撮像用孔216の突き当て面217aに突き当てて、先端硬質部材211に対する撮像ユニット300の位置決めを行うことができる。 Further, when assembling the imaging unit 300 to the distal end hard member 211, before the imaging unit 300 is inserted into the imaging hole 216, the imaging unit 300 is rotated about the axis, and each IG fiber of the IG bundle unit 320 is rotated. The resolution is adjusted due to the direction of alignment. The semi-tubular member 325 is attached to the IG bundle base 322 while maintaining the posture of the imaging unit 300 whose resolution has been adjusted, and the imaging unit 300 is inserted into the imaging hole 216 from the proximal end side of the distal end rigid member 211. insert. Accordingly, the imaging unit 300 can be positioned with respect to the distal end hard member 211 by abutting the distal end side end surface 325a of the semi-tubular member 325 against the abutting surface 217a of the imaging hole 216 while ensuring a desired resolution. .
 本発明に係る内視鏡は、先端硬質部材の先端側の細径化を図りつつ、先端硬質部材に対する撮像ユニットの位置決めを行うのに有用である。 The endoscope according to the present invention is useful for positioning the imaging unit with respect to the hard tip member while reducing the diameter of the hard tip member.
 1 内視鏡システム
 2 超音波内視鏡
 3 超音波観測装置
 4 内視鏡観察装置
 5 表示装置
 6 光源装置
 7 超音波振動子
 21 挿入部
 22 操作部
 23 ユニバーサルコード
 24 コネクタ
 31 超音波ケーブル
 41 ビデオケーブル
 211 先端硬質部材
 212 湾曲部
 213 可撓管部
 214 超音波振動子モジュール
 215 内視鏡モジュール
 215a 照明用レンズ
 215b 観察窓
 215c 処置具突出口
 216 撮像用孔
 217,218 溝部
 217a,218a 突き当て面
 219 処置具用挿通路
 219a 屈曲部
 221 湾曲ノブ
 222 操作部材
 223 処置具挿入口
 241 第1コネクタ部
 242 第2コネクタ部
 243 第3コネクタ部
 300 撮像ユニット
 310 レンズユニット
 311,312 対物レンズ
 313 レンズ枠
 314 突き当て部
 314a 先端側端面
 320 イメージガイドバンドルユニット
 321 イメージガイドバンドル
 322 IGバンドル口金
 323 軟性チューブ
 324 Cリング
 325 半管状部材
 326 角柱形状部材
 327 逆凹形状部材
DESCRIPTION OF SYMBOLS 1 Endoscope system 2 Ultrasound endoscope 3 Ultrasound observation apparatus 4 Endoscope observation apparatus 5 Display apparatus 6 Light source apparatus 7 Ultrasonic vibrator 21 Insertion part 22 Operation part 23 Universal code 24 Connector 31 Ultrasound cable 41 Video Cable 211 Hard end member 212 Curved portion 213 Flexible tube portion 214 Ultrasonic transducer module 215 Endoscope module 215a Illumination lens 215b Observation window 215c Treatment tool protrusion 216 Imaging hole 217, 218 Groove 217a, 218a Abutting surface 219 Treatment tool insertion path 219a Bending portion 221 Bending knob 222 Operation member 223 Treatment tool insertion port 241 First connector portion 242 Second connector portion 243 Third connector portion 300 Imaging unit 310 Lens unit 311, 312 Objective lens 313 Lens frame 314 Sudden Stopping portion 314a End side end surface 320 Image guide bundle unit 321 Image guide bundle 322 IG bundle base 323 Soft tube 324 C ring 325 Semi-tubular member 326 Square columnar member 327 Reverse concave shape member

Claims (6)

  1.  レンズユニットと画像伝送ユニットとを有し、被検体を撮像する撮像ユニットと、
     前記被検体内に挿入される挿入部の先端部分に設けられ、該被検体に対して所定の処置を施す処置具が挿通される処置具用挿通路と、前記撮像ユニットが配設される撮像用孔とが形成され、該撮像用孔の基端側に溝部が設けられた先端硬質部材と、
     前記撮像ユニットの前記先端硬質部材内における基端側に設けられ、前記溝部の先端側端面と突き当たる突き当て部と、
     を備えることを特徴とする内視鏡。
    An imaging unit having a lens unit and an image transmission unit, and imaging a subject;
    A treatment instrument insertion path that is provided at a distal end portion of an insertion portion that is inserted into the subject and that performs a predetermined treatment on the subject, and an imaging in which the imaging unit is disposed. A distal end hard member formed with a groove on the proximal end side of the imaging hole,
    An abutting portion provided on the proximal end side in the distal end hard member of the imaging unit, and abutting against the distal end side end surface of the groove;
    An endoscope comprising:
  2.  前記画像伝送ユニットは、画像伝送部材と、該画像伝送部材の先端側に設けられた口金とを有しており、
     前記口金とは別体で前記突き当て部を該口金の外周面に設けたことを特徴とする請求項1に記載の内視鏡。
    The image transmission unit has an image transmission member and a base provided on the tip side of the image transmission member,
    The endoscope according to claim 1, wherein the abutting portion is provided separately from the base and is provided on an outer peripheral surface of the base.
  3.  前記突き当て部はCリングであることを特徴とする請求項2に記載の内視鏡。 The endoscope according to claim 2, wherein the abutting portion is a C-ring.
  4.  前記口金に対して前記Cリングが接着によって固定されていることを特徴とする請求項3に記載の内視鏡。 The endoscope according to claim 3, wherein the C-ring is fixed to the base by adhesion.
  5.  前記画像伝送部材は、複数のイメージガイドファイバが束ねられたイメージガイドバンドル、または、撮像素子と信号線とで構成されることを特徴とする請求項2乃至4のいずれか1つに記載の内視鏡。 5. The image transmission member according to claim 2, wherein the image transmission member includes an image guide bundle in which a plurality of image guide fibers are bundled, or an imaging element and a signal line. Endoscope.
  6.  前記先端硬質部材の前記撮像用孔と前記処置具用挿通路との間の肉厚が、該先端硬質部材の軸線方向で先端側から基端側にかけて変化しており、前記肉厚が最も薄い箇所よりも基端側に前記溝部の先端側端面が位置することを特徴とする請求項1乃至5のいずれか1つに記載の内視鏡。 The wall thickness between the imaging hole of the distal rigid member and the treatment instrument insertion passage changes from the distal end side to the proximal end side in the axial direction of the distal rigid member, and the thickness is thinnest. The endoscope according to any one of claims 1 to 5, wherein a distal end side end face of the groove portion is located on a proximal end side with respect to the place.
PCT/JP2018/019596 2017-06-12 2018-05-22 Endoscope WO2018230274A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US16/708,716 US20200107708A1 (en) 2017-06-12 2019-12-10 Endoscope

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2017115316A JP2019000161A (en) 2017-06-12 2017-06-12 Endoscope
JP2017-115316 2017-06-12

Related Child Applications (1)

Application Number Title Priority Date Filing Date
US16/708,716 Continuation US20200107708A1 (en) 2017-06-12 2019-12-10 Endoscope

Publications (1)

Publication Number Publication Date
WO2018230274A1 true WO2018230274A1 (en) 2018-12-20

Family

ID=64660000

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/JP2018/019596 WO2018230274A1 (en) 2017-06-12 2018-05-22 Endoscope

Country Status (3)

Country Link
US (1) US20200107708A1 (en)
JP (1) JP2019000161A (en)
WO (1) WO2018230274A1 (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111065309B (en) * 2017-09-01 2022-05-24 奥林巴斯株式会社 Insertion part of endoscope
WO2022014999A1 (en) * 2020-07-13 2022-01-20 연세대학교 원주산학협력단 Endoscopic image diagnosis device having disposable ultrasound probe
JP7317778B2 (en) 2020-09-08 2023-07-31 富士フイルム株式会社 ultrasound bronchoscope

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2004135937A (en) * 2002-10-18 2004-05-13 Fuji Photo Optical Co Ltd Ultrasonic endoscope
WO2014034191A1 (en) * 2012-08-27 2014-03-06 オリンパスメディカルシステムズ株式会社 Ultrasonic endoscope
WO2014208218A1 (en) * 2013-06-25 2014-12-31 オリンパスメディカルシステムズ株式会社 Endoscope

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH04137309U (en) * 1991-06-14 1992-12-21 株式会社東芝 Photoelectric element module
SE511944C2 (en) * 1997-06-18 1999-12-20 Ericsson Telefon Ab L M Method of targeting optical building elements, carriers and optical components
JP3869528B2 (en) * 1997-07-03 2007-01-17 オリンパス株式会社 Endoscope
JP2011067384A (en) * 2009-09-25 2011-04-07 Fujifilm Corp Connector used to manufacture flexible tube for endoscope and method of manufacturing flexible tube for endoscope
JP5714121B2 (en) * 2012-04-17 2015-05-07 スガツネ工業株式会社 caster
JP6465300B2 (en) * 2015-06-17 2019-02-06 オリンパス株式会社 Endoscope

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2004135937A (en) * 2002-10-18 2004-05-13 Fuji Photo Optical Co Ltd Ultrasonic endoscope
WO2014034191A1 (en) * 2012-08-27 2014-03-06 オリンパスメディカルシステムズ株式会社 Ultrasonic endoscope
WO2014208218A1 (en) * 2013-06-25 2014-12-31 オリンパスメディカルシステムズ株式会社 Endoscope

Also Published As

Publication number Publication date
JP2019000161A (en) 2019-01-10
US20200107708A1 (en) 2020-04-09

Similar Documents

Publication Publication Date Title
EP1614390B1 (en) Ultrasonic endoscope
JP4618410B2 (en) Ultrasound endoscope
WO2018230274A1 (en) Endoscope
WO2017061537A1 (en) Ultrasonic endoscope
JP4725162B2 (en) Ultrasound endoscope
EP3323351A1 (en) Ultrasonic transducer module and ultrasonic endoscope
CN108778144B (en) Endoscope with a detachable handle
JP6197145B2 (en) Ultrasound endoscope
US10463238B2 (en) Endoscope and hard member
JP7249788B2 (en) Endoscope
JP6850694B2 (en) Endoscope and manufacturing method of endoscope
US20180098688A1 (en) Lens unit and endoscope
JP7223871B2 (en) ultrasound endoscope
JP7219580B2 (en) Ultrasonic endoscope and method for manufacturing ultrasonic endoscope
JP4488203B2 (en) Ultrasound endoscope
JP2019041884A (en) Ultrasonic endoscope
JP2017074231A (en) Method of manufacturing ultrasonic endoscope and ultrasonic endoscope
US11076744B2 (en) Method of manufacturing endoscope and endoscope
WO2021255903A1 (en) Endoscope
JP2023128309A (en) Endoscope
WO2020152791A1 (en) Ultrasound endoscope and endoscope system
JP4535252B2 (en) Ultrasound endoscope
JP2006158481A (en) Ultrasonic endoscope
JP2017225746A (en) Endoscope

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 18817578

Country of ref document: EP

Kind code of ref document: A1

NENP Non-entry into the national phase

Ref country code: DE

122 Ep: pct application non-entry in european phase

Ref document number: 18817578

Country of ref document: EP

Kind code of ref document: A1